ABSTRACT:
This a model from the article:
A metabolite-sensitive, thermodynamically constrained model of cardiac
cross-bridge cycling: implications for force development during ischemia.
Tran K, Smith NP, Loiselle DS, Crampin EJ. Biophys J
2010 Jan 20;98(2):267-76 20338848
,
Abstract:
We present a metabolically regulated model of cardiac active force generation
with which we investigate the effects of ischemia on maximum force production.
Our model, based on a model of cross-bridge kinetics that was developed by
others, reproduces many of the observed effects of MgATP, MgADP, Pi, and H(+) on
force development while retaining the force/length/Ca(2+) properties of the
original model. We introduce three new parameters to account for the competitive
binding of H(+) to the Ca(2+) binding site on troponin C and the binding of
MgADP within the cross-bridge cycle. These parameters, along with the Pi and
H(+) regulatory steps within the cross-bridge cycle, were constrained using data
from the literature and validated using a range of metabolic and sinusoidal
length perturbation protocols. The placement of the MgADP binding step between
two strongly-bound and force-generating states leads to the emergence of an
unexpected effect on the force-MgADP curve, where the trend of the relationship
(positive or negative) depends on the concentrations of the other metabolites
and [H(+)]. The model is used to investigate the sensitivity of maximum force
production to changes in metabolite concentrations during the development of
ischemia. Copyright 2010 Biophysical Society. Published by Elsevier Inc. All
rights reserved.
This model was taken from the CellML repository
and automatically converted to SBML.
The original model was:
Tran K, Smith NP, Loiselle DS, Crampin EJ. (2009) - version=1.0
The original CellML model was created by:
Catherine Lloyd
c.lloyd@auckland.ac.nz
The University of Auckland
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